510(k) K915565
K915565 is an FDA 510(k) premarket notification submitted by Tnt Moborg Intl. , Ltd. for the device "IMMOBILE". The FDA issued a decision of Substantially Equivalent on March 2, 1992. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Tnt Moborg Intl. , Ltd. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 2, 1992
- Date Received
- December 12, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tape And Bandage, Adhesive
- Device Class
- Class I
- Regulation Number
- 880.5240
- Review Panel
- SU
- Submission Type